FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NEUROMED TS8 TEST STIMULATOR

K Number: K903814 · Decision Jan 16, 1991
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
138
Applicant Total
15
Review Days
149

Basic Information

Device Name
NEUROMED TS8 TEST STIMULATOR
K Number
K903814
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5880
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
NEUROMED, INC.
Date Received
August 20, 1990
Decision Date
January 16, 1991
Product Code
GZB
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)

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Other Clearances by NEUROMED, INC.

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K930498 NEUROMED OCTRODE MODEL MNT-98 NEUROSTIMULATOR TRAN
K930242 INTRODE INT-8
K921319 NEUROMED MODEL OCA-30 OCTODE AND MODEL SCA-30
K905596 NEUROMED OCTRODE MODEL MNR-88B/88C NEUROSTIM SYST
K905255 NEUROMED MODEL 1992 LS LAMITRODE LEAD
K901499 NEUROMED OCTRODE MODEL MNR-88 W/98 ADAPTER NEURO.
K862915 MULTISTIM(4-CHANNEL), MULTISTIM-OCTRODE(8 CHANNEL)
K860185 UNISTIM UNT-1M NEUROSTIMULATOR TRANSMITTER
Search all 15 clearances from NEUROMED, INC. →